Skip to main content

Prevention of Microbial Contamination in Manufacturing

Prevention of Microbial Contamination in Manufacturing

Manufacturing area in pharmaceuticals must be contamination free and all personnel working in area should take care about the hygienic conditions to protect the product being manufactured.

The quality and safety of pharmaceutical products should be a key concern to any manufacturer in order to take care of clients consuming the product as well as maintaining their brand name in the market. Therefore to prevent microbial contamination in pharmaceutical products, there are some key measures or considerations that a manufacturer needs to take care of.

Manufacturers need to consider the building requirements such as windows which should be sealed properly to prevent microbial contamination or dust from being collected. The interior surfaces such as walls, floors or ceilings should not have cracks to prevent microbial contamination from getting in and also it allows cleaning to be easy and effective. The light points, as well as ventilation, should also be good to enable the cleaning of all areas well.

The sinks used in the production areas should be of stainless steel to prevent rusting that may contaminate the pharmaceutical product that is being manufactured. Utensils used and transfer lines in manufacturing should be made up of stainless steel only.

Another key consideration is facility design. This is done to ensure the flow of production is done effectively and run smoothly. For instance, to ensure the room is clean, air filtration and air change rates should be set. Also in the critical areas, the flow of air should be in one direction with sufficient velocity in order to prevent the particles from closing the area. The temperature, as well as humidity, should be regulated.

In case of any contaminants are being generated in the area, there should be an efficiently working HVAC system to remove and prevent the contaminants from spreading to other areas. Finally, ventilation dampers and other services should be positioned for maintenance purpose in a place away from the production area for easy access.

Personnel should also be considered in the prevention of microbial contamination in pharmaceuticals. Every person working in the production area should maintain high-level hygiene. Also, the people handling the production should be trained on the importance of hygiene and should wear protective clothing such as hair cover, overshoes, overgarments and beard cover which are appropriate during the operations to prevent contamination. They must avoid direct contact with the product or any part of the equipment that may have contact with the product. Finally, access to the area where production is taking place should be controlled and only trained people should be allowed.

Utilities used in the production of pharmaceuticals such as water and steam should be carefully selected. For instance, h igh quality purified water having controlled microbial load should be used for pharmaceutical manufacturing. Cleaning and rinsing of the equipment must be done by purified water.

For cleaning and disinfection, cleaning agents should be of suitable grade to minimize any health risks. The area should also be cleaned and disinfected regularly. The equipment for cleaning should not have direct contact with the pharmaceutical product. The cleaning practice should be validated to ensure that the cleaning process is effective to control microbial contamination.

Everyone working in pharmaceutical manufacturing should take care of preventing contamination. Visitors, as well as the personnel of other departments, should also be trained for working in the classified manufacturing area. The equipment carried out from the out site could be a source of microbial contamination, therefore, those should be cleaned and disinfected.

Comments

Popular posts from this blog

SOP for Washing of HPLC Column After Use

SOP for Washing of HPLC Column After Use Standard operating procedure to wash the HPLC column after analysis. 1.0 OBJECTIVE To clean the column thoroughly after its each use to avoid any interference on repeated usage. 2.0 SCOPE This procedure is applicable for different groups of H.P.L.C columns used in Quality Control laboratory. 3.0 RESPONSIBILITY 2.1 Doing: Technical Assistant 2.2 Checking: Executive /Manager 4.0 ACCOUNTABILITY Head of the Department 5.0 PROCEDURE 5.1 For C18, C8, C6, Phenyl, (CN, Amine, Silica column.:) 5.1.1 Wash the column with the solvent which is use in individual product mobile phase preparation. eg. suppose water is use in mobile phase  preparation then wash the column with water. 5.1.2 Allow the minimum 30 ml washing medium to flow through the column. 5.1.3 Disconnect the column from the HPLC unit and store in an allocated place. 5.2 For Protein pack column: 5.2.1 Wash the column with minimum 30 ml of 2.5 M acetic acid. 5.2.4 Disconnect the column from ...

Sterility Testing by Direct Inoculation Method

Sterility Testing by Direct Inoculation Method Direct Inoculation Method Learn the procedure for sterility test for sterile pharmaceutical products by direct inoculation method. 1.0 Objective :  To lay down Standard Operating Procedure is to provide guidelines for sterility testing by Direct Inoculation Method. 2.0 Scope This procedure is applicable for the products manufactured at the location which can not be tested by Membrane Filtration Method. 3.0 Responsibility Implementation: Microbiologist 4.0 Accountability Execution: Manager - QC Review & Approval : AGM - QA / QC Procedure Direct Inoculation Method Sample for Finished Products: Collect the samples to be tested for sterility. Out of the whole sample, randomly select 20 articles of each lot of batch for both LVP and SVP t erminal ly sterilized products and for aseptically filled products.    Sample for Intermediates: Randomly collect 16 pre-sterilized bottle samples to be tested for sterility from LVP bot...

Blow Fill Seal (BFS) and Form Fill Seal (FFS) Technology in Sterile Manufacturing

Blow Fill Seal (BFS) and Form Fill Seal (FFS) Technology in Sterile Manufacturing Know about sterile pharmaceutical production using Blow Fill Seal (BFS) and Form Fill Seal (FFS) technology. Both of these techniques are used to manufacture  sterile pharmaceutical products   as parenteral (LVP & SVP), infusions, ophthalmic and inhalation products. These are automated techniques to prepare sterile products. The basic concept of the  FFS   and BFS is to reduce the  contamination   by forming the container, filling and sealing in a closed sterile chamber of the machine. There is no personnel intervention to reduce the chances of the contamination during the manufacturing of sterile products. It gives more production at very low operational cost with the high assurance of  sterility . Blow fill seal technology is widely used and accepted by the various pharmaceutical regulatory authorities as US-FDA and MHRA. The system is being used for over 30 years a...

Aseptic Filling Process (Media Fill) Validation Protocol in Sterile Pharmaceuticals

Aseptic Filling Process (Media Fill) Validation Protocol in Sterile Pharmaceuticals Validation of sterile manufacturing process by media fill validation test as per PICS guidelines for aseptic validation or aseptic process simulation. 1.0 OBJECTIVE 1.1 To define procedures for validating and maintaining the validation of all aseptic filling processes and qualification of the quality of the product by system/facility/equipment. 2.0 SCOPE 2.1 This procedure applies to all aseptically filled sterile products intended for human use. 3.0 RESPONSIBILITY 3.1 The Validation personnel coordinate the aseptic filling validation program and write the sterile media aseptic filling processes reports. 3.2 Manufacturing personnel the sterile media aseptic filling processes and performs the sterile media fills. 3.3 QA personnel perform the sampling and assist with the IPQA monitoring required for each sterile media fill. 3.4 QC personnel to perform the testing and assist with the monitoring required fo...

Checklist for Audit in Sterile Area

Checklist for Audit in Sterile Area Checklist to verify the sterile manufacturing area before the audit. 1. Is there any SOP giving details for activity/ movement in the sterile area. 2. Verify the suitability of system for sanitization of hands. 3. Is there the SOP on entry-exit; gowning and de-gowning into the critical area available? 4. Verify the availability of following records:  Air pressure differential  Particulate monitoring  Temperature  Humidity  Microbiological monitoring by settle plate 5. Are these records available and maintained as per SOPs? 6. Check the above mentioned individual records. Are the entries within specifications mentioned in SOP/ MTPs. 7. Is the controlled copy of MTP pertaining to monitoring by settle plate available to plant person? 8. Are the location for settle plates identified and the chart/ layout available with plant? 9. Are the following areas monitored for parameters mentioned in step 4:  Air-lock to the critical ar...